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OncoMatch/Clinical Trials/NCT06751134

Chimeric Natural Killer Receptor-Universal T Cells for Relapsed or Refractory Neuroblastoma

Is NCT06751134 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies Chimeric Natural Killer Receptor Universal T-cells (CNK-UT) for neuroblastoma, recurrent, refractory.

Phase 1RecruitingNanjing Children's HospitalNCT06751134Data as of May 2026

Treatment: Chimeric Natural Killer Receptor Universal T-cells (CNK-UT)This is a single arm, open-label, multi-center, pilot studies (Investigator Initiated Trial, IIT) to evaluate the safety, preliminary efficacy, pharmacokinetics of universal T-cells engineered with chimeric natural killer receptor (CNK-UT) to treat the patients with relapsed/refractory Neuroblastoma.

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Extracted eligibility criteria

Cancer type

Neuroblastoma

Biomarker criteria

Required: CD276 expression (positive by ihc)

Prior therapy

Must have received: induction chemotherapy — first-line

standard treatment protocols, which include induction chemotherapy, surgery, and radiotherapy targeting the primary tumor and residual metastatic sites

Must have received: surgery — first-line

standard treatment protocols, which include induction chemotherapy, surgery, and radiotherapy targeting the primary tumor and residual metastatic sites

Must have received: radiation therapy — first-line

standard treatment protocols, which include induction chemotherapy, surgery, and radiotherapy targeting the primary tumor and residual metastatic sites

Cannot have received: gene therapy

Participants who have used any gene therapy products prior to cell infusion

Lab requirements

Blood counts

ANC≥1.5×10^9/L; ALC≥0.2×10^9/L; Platelet count ≥75×10^9/L; Haemoglobin≥90g/L

Kidney function

Serum creatinine≤2×ULN, or Creatinine clearance rate (CCR)≥60 mL/min (Cockroft-Gault formula)

Liver function

Total bilirubin≤3×ULN; AST or ALT≤5×ULN

Cardiac function

LVEF≥50%; Cardiac function Grade I-II

Adequate organ and bone marrow function, and the laboratory test value meets the following requirements within 7 days before enrollment, as follows: (1)Blood Routine Test: Absolute neutrophil count(ANC)≥1.5×10^9/L;Absolute lymphocyte count (ALC)≥0.2×10^9/L;Platelet count ≥75×10^9/L; Haemoglobin≥90g/L; (2)Heart: Left ventricular ejection fraction (LVEF)≥50%;Cardiac function Grade I-II; (3)Pulmonary function: indoor oxygen saturation≥92%. (4)Hepatic function:Total bilirubin≤3×ULN; Aspartate aminotransferase (AST) or alanine aminotransferase (ALT)≤5×ULN; (5)Renal function: Serum creatinine≤2×ULN, or Creatinine clearance rate (CCR)≥60 mL/min (Cockroft-Gault formula);

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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